This page is part of the FHIR Specification (v3.0.2: STU 3). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3
Clinical Genomics Work Group | Maturity Level: N/A | Ballot Status: Informative | Compartments: Not linked to any defined compartments |
This is the narrative for the resource. See also the XML or JSON format. This example conforms to the profile Sequence.
Generated Narrative with Details
id: fda-example
type: dna
coordinateSystem: 1
patient: Patient/example
- | ReferenceSeqId | Strand | WindowStart | WindowEnd |
* | NC_000001.11 (Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NC_000001.11' = 'NC_000001.11) | 1 | 10453 | 101770080 |
- | Start | End | ObservedAllele | ReferenceAllele |
* | 13116 | 13117 | T | G |
- | Type | StandardSequence | Start | End | Method | TruthTP | QueryTP | TruthFN | QueryFP | GtFP | Precision | Recall | FScore |
* | snp | file-Bk50V4Q0qVb65P0v2VPbfYPZ (Details : {https://precision.fda.gov/files/ code 'file-Bk50V4Q0qVb65P0v2VPbfYPZ' = 'file-Bk50V4Q0qVb65P0v2VPbfYPZ) | 10453 | 101770080 | Vcfeval + Hap.py Comparison (Details : {https://precision.fda.gov/jobs/ code 'job-ByxYPx809jFVy21KJG74Jg3Y' = 'job-ByxYPx809jFVy21KJG74Jg3Y) | 7749 | 7984 | 2554 | 10670 | 2186 | 0.428005 | 0.752111 | 0.545551 |
- | Type | Url | Name | VariantsetId |
* | login | https://precision.fda.gov/files/file-Bx37ZK009P4bX5g3qjkFZV38 | FDA | file-Bx37ZK009P4bX5g3qjkFZV38 |
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.